A non-dense sintered ceramic molded body having at least two layers, wherein a first powdery ceramic material forming a layer is contacted with at least a second powdery material forming at least a second layer. The body has a color gradient and maintains dimensional stability during sintering and forming. An admixing component and a common sintering temperature are used to control the volume decrease of the layers during sintering.
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1. A sintered ceramic molded body for dental purposes comprising a continuous color gradient and at least two layers, obtainable by a process,
wherein a first powdery ceramic material forming a layer is contacted with at least a second powdery ceramic material forming at least a second layer;
said first powdery ceramic material has a presintering temperature t1 that is higher than the presintering temperature t2 of said at least second powdery ceramic material;
said at least second powdery ceramic material exhibiting a more intense coloring than that of the first powdery ceramic material as evaluated with the CIE-Lab color system;
the course of a curve of shrinkage S1 of said at least first powdery ceramic material differs from the course of a curve of shrinkage S2 of said at least second powdery ceramic material, wherein curve of shrinkage S1 is shifted towards higher temperatures as compared to curve of shrinkage S2; and
wherein the curve of shrinkage S1 is shifted toward lower temperatures by admixing the first powdery ceramic material with at least one component that has a curve of shrinkage S3 and a presintering temperature t3 and being compatible with said first powdery ceramic material wherein the at least one component material has a grain size smaller than the grain size of the first powdery ceramic material, to equalize the curves of shrinkage S1 and S2 in the region of a presintering temperature tS with tS being the presintering temperature at which the layers forming the molded body are subjected to a common temperature treatment to form a porous sintered molded body, the admixed materials having a curve of shrinkage that is between the curves of shrinkage S1 and S3 in a region of tS; and
the layers are subjected to the common temperature treatment at tS to cause sintering that remains in a stage that has not proceeded to the theoretical density, tS being lower than t1 and at least equal to t3 with the layers showing no distortions that are due to sintering distortions after completion of common temperature treatment;
wherein the at least one component material comprises zirconia, and
wherein curves of shrinkage are measured under the same conditions.
3. The molded body according to any
5. The molded body according to
6. The molded body according to
7. The molded body of
8. The molded body of
9. The molded body of
10. The molded body of
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This application is a divisional application of copending U.S. patent application Ser. No. 14/391,042 to Dorn et al., entitled “Process for Producing a Non-Dense Sintered Ceramic Molded Body Having at Least Two Layers” which is a national stage filing of PCT Application No. PCT/EP2013/057917, which claims priority to European Patent Application No. 12164282.1 filed Apr. 16, 2012 and to U.S. Provisional Application No. 61/644,055 filed May 8, 2012, each of which are incorporated herein by reference.
The present invention relates to a process for producing a non-dense sintered ceramic molded body having at least two layers and to a molded body obtainable by the process according to the invention.
The use of glass-ceramic restorations has proven effective for the restoration of dental defects, especially in the region of the mouth. Because of the low strength of such restorations as compared to those made of stabilized zirconia, these materials, which meet aesthetic requirements, are not indicated for the preparation of bridges or for restoring patients suffering from masticatory disorders (bruxism). For the preparation of posterior bridges or crowns, it has been usual to produce scaffolds of a high strength material, which subsequently need to be faced with a glass ceramic layer. If fully anatomical crowns or minimally reduced crowns are to be produced by CAD/CAM technologies, the blanks obtained are only glazed or provided with a thin veneer layer. This is an alternative to a cast crown and is not to be recognized as a restoration if possible. However, this requires that the crown is not unicolored, but has a multicolored design, a color gradient running from the tooth neck towards the incisal edge/occlusal surface from dark to light in order to reproduce the color gradient of a natural tooth as exactly as possible.
Articles made of zirconia, especially for dental purposes, have become established because of their comparatively high bending strength. However, the common zirconia materials for dental purposes are unicolored and can be immediately recognized as a restoration because of their light color. Therefore, copings for crowning prepared therefrom must always be faced in order that the restoration fits aesthetically into the remaining teeth. In order to achieve a natural coloring, porous monolithic zirconia restorations, which may also have been precolored in a single color, are matched with coloring liquids to the individual situation in the patient.
EP 1 859 757 A discloses ZrO2-based compositions as well as unicolored and multicolored blanks made of oxide ceramics, and a process for the preparation thereof, in which a) oxide-ceramic powders are coated with a coloring substance, b) the coated powders are preferably classified, and at least one colored powder is filled into a compression mold, c) the colored powder or powders is/are compressed into a molded body, and d) the compressed molded body is sintered into a blank, and the use of such blanks for preparing dental restorations.
EP 1 859 758 A discloses a block body of ceramic compositions, especially feldspar-based dental compositions, consisting of at least one ceramic composition with predefined first optical properties and at least one second ceramic composition with predefined second optical properties, and a transition zone between the two ceramic compositions constituted of varying blends of said at least two ceramic compositions, the variation gradient of the blends being essentially constant.
EP 1 900 341 A discloses a multicolored molded body, especially made of feldspar ceramics, with superimposed layers for preparing dental prostheses, at least two successive layers of different colors and at least two intermediate layers of different colors between at least two successive primary layers of different colors, wherein between these intermediate layers a change of the color takes place along a direction that is opposite to the direction of the change in color between the primary layers.
WO 2007/137696A discloses green body consisting of at least two different molding powder mixtures each containing a ceramic powder, and a coloring metal compound and/or a coloring pigment which are compressed to form the green body. The green body ceramics are particularly suitable as color-graded dental ceramics (blanks), which serve as all-ceramic restorations. The powder mixtures can consist out of a zirconia granulate and a zirconium silicate material, in which the zirconium silicate changes the chemical structure and lowers the mechanical properties (e.g. 3-point bending strength).
Iron oxides, for example, are used for coloring zirconia granules. These or similar additives influence the sintering behavior because they change the sintering activity. Thus, a more intensely colored region can differ from a less intensely colored region in terms of shrinkage or density at the same temperature. This deviating sintering behavior unavoidably provokes deformation of the original geometry, if the sintering process is stopped before the theoretical density is reached, in favor of improved processability.
Mixing pigmented and non-pigmented zirconia granules basically enables the preparation of a color-layered geometry or the production of a three-dimensional gradient. For processing by CAD/CAM technology, it is necessary that such blocks or disks are presintered at a particular temperature in order to ensure good grindability. The presintering essentially corresponds to an intermediate stage on the way to the final dense sintering, as close as possible to the theoretical density. However, the presintering of multicolored blocks is problematic because a sintering distortion between lighter and darker regions occurs in the mentioned intermediate stage. This distortion is caused by different sintering activities, which are primarily due to the proportion of coloring components. However, since the final sintering density of the layers as achieved in dense sintering is almost identical, the ground object would again become distorted from the intermediate stage to the final stage.
To date, no solutions have been known that enable the production of a color gradient in zirconia blanks in such a way that they can be subsequently processed in a porous sintered state.
Indeed, it would be basically possible to circumvent the difficulties by determining the sintering distortion in advance and calculating a correction during the processing by CAM software. However, this method would reach the limits of travel paths of the CAM machines when there are undercuts, and therefore is not workable in practice. Also, this method does not achieve the object of the invention.
It is desirable to adjust colored and colorless powders or granules of zirconia in such a way that they do not exhibit distortion in the processable intermediate stage and in the final density, i.e., after processing and dense sintering.
The object of the invention is achieved by a process for producing a non-dense sintered ceramic molded body having at least two layers,
An advantage of the process according to the invention resides in the fact, among others, that the relevant properties of a known material are maintained while the optical properties can be controlled in a desired direction. Thus, for example, it is possible to design the block with differently colored layers in almost any number. Further, it is also possible to produce a multicolored block by continuous mixing methods and by using just a few starting colors, wherein the color grading may also be a continuous gradient.
The process according to the invention enables the coloring of yttrium-stabilized zirconium layers, which can be arranged as superimposed blocks. Thus, the user gets the possibility to use for restorations made of zirconia respectively the same starting material that has already been largely used for unicolored dental prostheses or dental replacement scaffolds. The physical properties remain essentially unchanged as compared to the established product. Disturbing or time-consuming operations, such as the coloring of the scaffolds or the facing of the scaffolds, can be reduced to a minimum or are superfluous. Color variations in the restoration to be produced can be defined by a simulation with the software designated for the processing. After the CAD/CAM production off the restoration, the sintering process performed to dense sintering, a glaze layer can be applied if desired.
In one embodiment of the process according to the invention, the first powdery ceramic material contains yttrium-stabilized zirconia, which is commercially available, for example, as granules from the company TOSOH, Japan, under the designation TZ-3YSB-C(Curve S1, T1).
In a further embodiment of the process according to the invention, the at least second powdery ceramic material contains yttrium-stabilized zirconia that exhibits a more intense coloring than that of the first powdery ceramic material. The at least second powdery ceramic material is commercially available, for example, as granules from the company TOSOH, Japan, under the designation TZ-Yellow-SB-C. (Curve S2, TS)
In another embodiment of the process according to the invention, the component admixed into the first powdery ceramic material is, for example, the granules obtainable from the company TOSOH, Japan, under the designation TZ-PX-242A or Zpex (Curve S3, T3).
In particular, the presintering temperature T1 according to the present invention is within a range of from 900° C. to 1300° C., especially from 950° C. to 1150° C., from 1000° C. to 1100° C., or from 1040° C. to 1080° C., TS is within a range of from 850° C. to 1250° C., and/or T3 is within a range of from 800° C. to 1200° C.
The invention is explained in more detail in the following.
For example, the first powdery ceramic material is white or only weakly colored, and the second powdery ceramic material represents a more intensely couloured powdery ceramic material having a grain size in the range of the first powdery ceramic material. The third curve S3 has a smaller grain size than the first powdery ceramic material. The curves of shrinkage S1 and S2 of the two powdery ceramic ground materials are so much different that the disadvantageous distortions of the first and second layers occur.
Surprisingly, admixing a component with a curve of shrinkage S3 compatible with the first powdery ceramic material to the first powdery ceramic material can equalize its curve of shrinkage S1 to the curve of shrinkage S2 of the second powdery ceramic material within the range of the selected presintering temperature, or even achieve identical curves of shrinkage. The shifting of the curve of shrinkage S1 depends on the level of admixing the component compatible with the first powdery ceramic material. The compatibility of the component with curve S3 is related with its smaller grain size compared with the first powdery ceramic material. In particular the difference in grain size of the two materials is at least 5%, more particularly 10% or 20% or even 30% or more such as 40%.
Said component compatible with the first powdery ceramic material may be, for example, a zirconia material containing, in addition to yttria in the percent range, especially 6-7%: less than one percent of alumina, traces of silica, and iron oxide as a pigment, wherein less alumina is present as compared to the first powdery ceramic material. The particle size of the component is smaller than that of the first powdery ceramic material, and typically the size of the particles of the component is about half the size of the particles of the first powdery ceramic material, whose particle size is within a range of 80-100 nm. The BET value of the component to be admixed is about double the BET value of the first powdery ceramic material. Typical BET values for the component to be admixed are 11-15 m2/g. Such materials are commercially available and are distributed under the designation TZ-PX-242A or Zpex from TOSOH, Japan, for the component to be admixed, and under the designation TZ-3YSB-C, TOSOH, Japan, for the first powdery ceramic material. The material forming component 2 is the at least second powdery ceramic material according to the present invention, being provided with a higher pigmentation, typically in the form of iron oxide, as compared to the first powdery ceramic material. Iron oxide has a yellowish color.
The following table shows properties of a special first and second powdery ceramic material.
TZ-PX-242A
TZ-3YSB-C
Crystallite Size [nm]
32
36
Particle size D50 [μm]
0.43
0.60
Granule Size [μm]
52
60
Bulk Density [g/cm3]
1.06
1.20
Specific surface area [m2/g]
ca. 12
ca. 6
The component compatible with the first powdery ceramic material is admixed with the first powdery ceramic material in proportions within a range of 25 percent by weight to 50 percent by weight (especially from 30 to 40% by weight) in order to achieve the effect of equalizing the curves of shrinkage as desired according to the invention.
The molded bodies according to the invention, which can be prepared by applying the process according to the invention, advantageously show no distortions that are due to sintering distortion after completion of the presintering, so that the molded body in this porous sintered state can be processed by material removal, and does not experience any deformation after dense sintering.
In a three-layer stacking in
The molded body according to the invention is advantageously prepared by intimately mixing the first powdery ceramic material with the component compatible with this material. The mixed material is filled into a mold, the forming layer is smoothed and then covered with a second layer of a mixture of component 1 and component 2. This step is repeated to form the third layer. The material is compacted under pressure (typically 100 to 200 MPa) and then released from the mold.
This is followed by a sintering process in which the temperature is raised. The temperature raise is stopped at a temperature selected in such a way that the molded body obtained can be readily machined, and subjected to dense sintering after processing. The presintering temperature is within a range of from 800° C. to 1200° C., especially from 950° C. to 1150° C., 1000-1100° C., or 1040-1080° C.
For facilitating the machining, the molded body according to the invention is provided with relevant elements known to the skilled person that are suitable for fixing the block within a CAD/CAM machine.
In a further embodiment of the process according to the invention, the porous sintered molded body obtained is further processed by forming processes.
The present invention also relates to a molded body obtainable by the process according to the invention. Advantageously, the layers are dimensionally stable in the porous sintering.
Component 1 is obtained by intimately mixing 650 g of TZ-3YSB-C from TOSOH, Japan (T1˜1076° C.), with 350 g of TZ-PX-242A from TOSOH, Japan (T3˜1038° C.), in a mixer from the company Bachofen, type DynaMix® CM200 (or CM100, CM500, CM1000). For forming by means of an axial compression method, component 1 is filled into the stamper by means of a filling unit known to the skilled person. The layer is uniformly spread in the mold by pulling away the filling unit. Typically, the layer thickness is higher than the desired layer thickness of the final product because of the bulk density being lower than the compressed density, and depends on the raw materials employed. Typically, the filled-in layer thickness of the powder is 2.318 times the corresponding layer thickness of the compressed component and is 14.88 mm. Onto this layer, 22.29 g of a mixture of 80% by weight component 1 and 20% by weight component 2, which consists of TZ-Yellow-SBC from TOSOH, Japan, is applied. After the second layer has been filled in, it is also smoothed and thereafter covered by the third layer consisting of the intimately mixed components 1 and 2 in a mixing ratio of 60% by weight to 40% by weight. Optionally, smoothing is again performed. Thereafter, the layered structure in the mold is compacted under a pressure of 200-165 MPa to a density of 3.13 g/cm3.
After the compressed molded body has been released, it is subjected to sintering until a temperature (TS) of 1060° C. is reached. The molded body can be processed into multi-unit bridges by means of CAD/CAM methods. The bridges obtained are dense sintered at temperatures of 1530° C.
The corresponding colors of the individual layers can be seen from
The sintered block is provided with a holding member. This is realized by adhesive-bonding the block and holding member. The porous ceramic component is placed by means of a centering device onto the holding member fixed in a base plate and provided with adhesive, and is thus fixed.
The blocks shown in
Layer 1
Layer 2
Layer 3
Block
Comp. 1 to
Comp. 1 to
Comp. 1 to
according
comp. 2
comp. 2
comp. 2
to
[% by weight]
[% by weight]
[% by weight]
FIG. 2B
80 to 20
60 to 40
40 to 60
FIG. 2C
60 to 40
40 to 60
20 to 80
FIG. 2D
40 to 60
20 to 80
0 to 100
The following Table illustrates the quantitative ranges in which the component compatible with the first powdery ceramic material can be mixed with the first powdery ceramic material in order to achieve the desired presintering temperature in the production process and to arrive at molded bodies that are according to the invention.
Proportion of
Proportion of
Proportion of
TZ-3YSB-C
TZ-PX-242A
TZ-Yellow-SB-C
in layer 1
in layer 1
in layer 2
Presintering
[% by
[% by
[% by
temperature
Example
weight]
weight]
weight]
[° C.]
1
70
30
100
1066
2
60
40
100
1066
3
50
50
100
1066
Thiel, Norbert, Tholey, Michael, Dorn, Michael, Godiker, Michael
| Patent | Priority | Assignee | Title |
| Patent | Priority | Assignee | Title |
| 4316964, | Jul 14 1980 | NORTON CO , A CORP OF DE | Al2 O3 /ZrO2 ceramic |
| 4431451, | Apr 22 1979 | AMERICAN DENTAL ASSOCAITION HEALTH FOUNDATION | Dental material |
| 4558018, | Apr 04 1983 | NGK Insulators, Ltd. | Silicon nitride sintered bodies and a method for producing the same |
| 4820667, | Aug 18 1986 | NGK Insulators, Ltd. | High strength zirconia ceramic |
| 5009597, | Mar 17 1987 | Kulzer & Co. GmbH | Composite dental prosthesis element formed of filled acrylate/methacrylate polymers |
| 5300324, | May 29 1992 | JPMORGAN CHASE BANK, N A , AS COLLATERAL AGENT | Process to increase the drying rate of a glaze for ceramics |
| 5578349, | Nov 30 1995 | Caterpillar Inc. | Process for coating a ceramic glow plug portion with a corrosion inhibiting material |
| 6022819, | Jul 17 1998 | ARDENT, INC | Dental porcelain compositions |
| 6576182, | Mar 31 1995 | NASS, RUEDIGER | Process for producing shrinkage-matched ceramic composites |
| 7056851, | Aug 22 2003 | PHC HOLDINGS CO , LTD ; PANASONIC HEALTHCARE HOLDINGS CO , LTD | ZrO2-Al2O3 composite ceramic material |
| 7229286, | Apr 20 2001 | NEW AGE BIOMATERIALS | Composite veneered cast glass-ceramic dental construct |
| 7399722, | Sep 10 2003 | Kyocera Corporation | Alumina/zirconia ceramics and method of producing the same |
| 20020031675, | |||
| 20040081765, | |||
| 20040232576, | |||
| 20110177424, | |||
| 20120034446, | |||
| 20130255850, | |||
| 20180063975, | |||
| CA1251305, | |||
| DE102006024489, | |||
| EP364281, | |||
| EP870479, | |||
| EP1510187, | |||
| EP1859757, | |||
| EP1859758, | |||
| EP1900341, | |||
| JP2002153492, | |||
| JP2004035322, | |||
| WO2076907, | |||
| WO2004009503, | |||
| WO2006120254, | |||
| WO2007028787, | |||
| WO2007137696, | |||
| WO2008106958, | |||
| WO2007137696, |
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